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Habitat Selection by Two K-Selected Species: an Application to Bison and Sage Grouse
Brigham Young University BYU ScholarsArchive Theses and Dissertations 2013-12-01 Habitat Selection by Two K-Selected Species: An Application to Bison and Sage Grouse Joshua Taft Kaze Brigham Young University - Provo Follow this and additional works at: https://scholarsarchive.byu.edu/etd Part of the Animal Sciences Commons BYU ScholarsArchive Citation Kaze, Joshua Taft, "Habitat Selection by Two K-Selected Species: An Application to Bison and Sage Grouse" (2013). Theses and Dissertations. 4284. https://scholarsarchive.byu.edu/etd/4284 This Thesis is brought to you for free and open access by BYU ScholarsArchive. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Habitat Selection by Two K-Selected Species: An Application to Bison and Sage-Grouse in Utah Joshua T. Kaze A thesis submitted to the faculty of Brigham Young University in partial fulfillment of the requirements for the degree of Masters of Science Randy T. Larsen, Chair Steven Peterson Rick Baxter Department of Plant and Wildlife Science Brigham Young University December 2013 Copyright © 2013 Joshua T. Kaze All Rights Reserved ABSTRACT Habitat Selection by Two K-Selected Species: An Application to Bison and Sage-Grouse in Utah Joshua T. Kaze Department of Plant and Wildlife Science, BYU Masters of Science Population growth for species with long lifespans and low reproductive rates (i.e., K- selected species) is influenced primarily by both survival of adult females and survival of young. Because survival of adults and young is influenced by habitat quality and resource availability, it is important for managers to understand factors that influence habitat selection during the period of reproduction. -
Predators As Agents of Selection and Diversification
diversity Review Predators as Agents of Selection and Diversification Jerald B. Johnson * and Mark C. Belk Evolutionary Ecology Laboratories, Department of Biology, Brigham Young University, Provo, UT 84602, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-801-422-4502 Received: 6 October 2020; Accepted: 29 October 2020; Published: 31 October 2020 Abstract: Predation is ubiquitous in nature and can be an important component of both ecological and evolutionary interactions. One of the most striking features of predators is how often they cause evolutionary diversification in natural systems. Here, we review several ways that this can occur, exploring empirical evidence and suggesting promising areas for future work. We also introduce several papers recently accepted in Diversity that demonstrate just how important and varied predation can be as an agent of natural selection. We conclude that there is still much to be done in this field, especially in areas where multiple predator species prey upon common prey, in certain taxonomic groups where we still know very little, and in an overall effort to actually quantify mortality rates and the strength of natural selection in the wild. Keywords: adaptation; mortality rates; natural selection; predation; prey 1. Introduction In the history of life, a key evolutionary innovation was the ability of some organisms to acquire energy and nutrients by killing and consuming other organisms [1–3]. This phenomenon of predation has evolved independently, multiple times across all known major lineages of life, both extinct and extant [1,2,4]. Quite simply, predators are ubiquitous agents of natural selection. Not surprisingly, prey species have evolved a variety of traits to avoid predation, including traits to avoid detection [4–6], to escape from predators [4,7], to withstand harm from attack [4], to deter predators [4,8], and to confuse or deceive predators [4,8]. -
Excretion of Zooplankton and Benthos
PART IV: ASSIMILAT ION EFF ICI ENCY, EGESTION, AND EXCRETION OF ZOOPLANKTON AND BENTHOS I ntroduction 203 . Assimilat ion (A) i s t he f ood absorbed f rom a n i ndividual 's digestive syst em. Assimilation efficiency (A/G) is the proportion o f co ns umption (G) actuall y ab sorbed (Sushchenya 1969 , Odum 19 71, Wetzel 1975 ) . Although the t e rm A/G i s usua lly used in reference t o i ndividual o r ga ni sms , it also can be app lied to popu lations. Ege stion i s food that is not ass imi lated by the gu t a nd whi ch is elimina ted as feces (Pe nna k 1964 ). By co n t r ast , excretion is a waste product formed from assimilated f ood a nd gener a l ly i s e l imi nated in a d i s s o l ved form. 204 . Energy f low refe r s t o the assimilat ion of a population and i s de signated a s t he s um of produ cti on (P) and r espiration (R) , i .e ., A = P + R (Sus hchenya 1969 ; Odum 1971) . The e fficiency o f energy flow in a popul ation, p ~ R , may be approx ima tely e qua l t o the a ssimi l a tion efficiency of an i nd i vidua l in t hat population (Sushchenya 1969) . However , since A/G o f t en de pends on age (Sch indler 1968, Waldbaue r 1968 , Winberg et al . -
Meiobenthos of the Discovery Bay Lagoon, Jamaica, with an Emphasis on Nematodes
Meiobenthos of the discovery Bay Lagoon, Jamaica, with an emphasis on nematodes. Edwards, Cassian The copyright of this thesis rests with the author and no quotation from it or information derived from it may be published without the prior written consent of the author For additional information about this publication click this link. https://qmro.qmul.ac.uk/jspui/handle/123456789/522 Information about this research object was correct at the time of download; we occasionally make corrections to records, please therefore check the published record when citing. For more information contact [email protected] UNIVERSITY OF LONDON SCHOOL OF BIOLOGICAL AND CHEMICAL SCIENCES Meiobenthos of The Discovery Bay Lagoon, Jamaica, with an emphasis on nematodes. Cassian Edwards A thesis submitted for the degree of Doctor of Philosophy March 2009 1 ABSTRACT Sediment granulometry, microphytobenthos and meiobenthos were investigated at five habitats (white and grey sands, backreef border, shallow and deep thalassinid ghost shrimp mounds) within the western lagoon at Discovery Bay, Jamaica. Habitats were ordinated into discrete stations based on sediment granulometry. Microphytobenthic chlorophyll-a ranged between 9.5- and 151.7 mg m -2 and was consistently highest at the grey sand habitat over three sampling occasions, but did not differ between the remaining habitats. It is suggested that the high microphytobenthic biomass in grey sands was related to upwelling of nutrient rich water from the nearby main bay, and the release and excretion of nutrients from sediments and burrowing heart urchins, respectively. Meiofauna abundance ranged from 284- to 5344 individuals 10 cm -2 and showed spatial differences depending on taxon. -
Seventh Grade
Name: _____________________ Maui Ocean Center Learning Worksheet Seventh Grade Our mission is to foster understanding, wonder and respect for Hawai‘i’s Marine Life. Based on benchmarks SC.6.3.1, SC. 7.3.1, SC. 7.3.2, SC. 7.5.4 Maui Ocean Center SEVENTH GRADE 1 Interdependent Relationships Relationships A food web (or chain) shows how each living thing gets its food. Some animals eat plants and some animals eat other animals. For example, a simple food chain links plants, cows (that eat plants), and humans (that eat cows). Each link in this chain is food for the next link. A food chain always starts with plant life and ends with an animal. Plants are called producers (they are also autotrophs) because they are able to use light energy from the sun to produce food (sugar) from carbon dioxide and water. Animals cannot make their own food so they must eat plants and/or other animals. They are called consumers (they are also heterotrophs). There are three groups of consumers. Animals that eat only plants are called herbivores. Animals that eat other animals are called carnivores. Animals and people who eat both animals and plants are called omnivores. Decomposers (bacteria and fungi) feed on decaying matter. These decomposers speed up the decaying process that releases minerals back into the food chain for absorption by plants as nutrients. Do you know why there are more herbivores than carnivores? In a food chain, energy is passed from one link to another. When a herbivore eats, only a fraction of the energy (that it gets from the plant food) becomes new body mass; the rest of the energy is lost as waste or used up (by the herbivore as it moves). -
Islands in the Stream 2002: Exploring Underwater Oases
Islands in the Stream 2002: Exploring Underwater Oases NOAA: Office of Ocean Exploration Mission Three: SUMMARY Discovery of New Resources with Pharmaceutical Potential (Pharmaceutical Discovery) Exploration of Vision and Bioluminescence in Deep-sea Benthos (Vision and Bioluminescence) Microscopic view of a Pachastrellidae sponge (front) and an example of benthic bioluminescence (back). August 16 - August 31, 2002 Shirley Pomponi, Co-Chief Scientist Tammy Frank, Co-Chief Scientist John Reed, Co-Chief Scientist Edie Widder, Co-Chief Scientist Pharmaceutical Discovery Vision and Bioluminescence Harbor Branch Oceanographic Institution Harbor Branch Oceanographic Institution ABSTRACT Harbor Branch Oceanographic Institution (HBOI) scientists continued their cutting-edge exploration searching for untapped sources of new drugs, examining the visual physiology of deep-sea benthos and characterizing the habitat in the South Atlantic Bight aboard the R/V Seaward Johnson from August 16-31, 2002. Over a half-dozen new species of sponges were recorded, which may provide scientists with information leading to the development of compounds used to study, treat, or diagnose human diseases. In addition, wondrous examples of bioluminescence and emission spectra were recorded, providing scientists with more data to help them understand how benthic organisms visualize their environment. New and creative Table of Contents ways to outreach and educate the public also Key Findings and Outcomes................................2 Rationale and Objectives ....................................4 -
Understanding Bioluminescence in Dinoflagellates—How Far Have We Come?
Microorganisms 2013, 1, 3-25; doi:10.3390/microorganisms1010003 OPEN ACCESS microorganisms ISSN 2076-2607 www.mdpi.com/journal/microorganisms Review Understanding Bioluminescence in Dinoflagellates—How Far Have We Come? Martha Valiadi 1,* and Debora Iglesias-Rodriguez 2 1 Department of Evolutionary Ecology, Max Planck Institute for Evolutionary Biology, August-Thienemann-Strasse, Plӧn 24306, Germany 2 Department of Ecology, Evolution and Marine Biology, University of California Santa Barbara, Santa Barbara, CA 93106, USA; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected] or [email protected]; Tel.: +49-4522-763277; Fax: +49-4522-763310. Received: 3 May 2013; in revised form: 20 August 2013 / Accepted: 24 August 2013 / Published: 5 September 2013 Abstract: Some dinoflagellates possess the remarkable genetic, biochemical, and cellular machinery to produce bioluminescence. Bioluminescent species appear to be ubiquitous in surface waters globally and include numerous cosmopolitan and harmful taxa. Nevertheless, bioluminescence remains an enigmatic topic in biology, particularly with regard to the organisms’ lifestyle. In this paper, we review the literature on the cellular mechanisms, molecular evolution, diversity, and ecology of bioluminescence in dinoflagellates, highlighting significant discoveries of the last quarter of a century. We identify significant gaps in our knowledge and conflicting information and propose some important research questions -
Benthic Invertebrate Bycatch from a Deep-Water Trawl Fishery, Chatham Rise, New Zealand
AQUATIC CONSERVATION: MARINE AND FRESHWATER ECOSYSTEMS, VOL. 7, 27±40 (1997) CASE STUDIES AND REVIEWS Benthic invertebrate bycatch from a deep-water trawl fishery, Chatham Rise, New Zealand P. KEITH PROBERT1, DON G. MCKNIGHT2 and SIMON L. GROVE1 1Department of Marine Science, University of Otago, PO Box 56, Dunedin, New Zealand 2National Institute of Water and Atmospheric Research Ltd, PO Box 14-901, Kilbirnie, Wellington, New Zealand ABSTRACT 1. Benthic invertebrate bycatch was collected during trawling for orange roughy (Hoplostethus atlanticus) at water depths of 662±1524 m on the northern and eastern Chatham Rise, New Zealand, in July 1994. Seventy-three trawl tows were examined, 49 from `flat' areas and 24 from two groups of `hills' (small seamounts). Benthos was recorded from 82% of all tows. 2. Some 96 benthic species were recorded including Ophiuroidea (12 spp.), Natantia (11 spp.), Asteroidea (11 spp.), Gorgonacea (11 spp.), Holothuroidea (7 spp.), and Porifera (6 spp.). 3. Cluster analysis showed the bycatch from flats and hills to differ significantly. Dominant taxa from flats were Holothuroidea, Asteroidea and Natantia; whereas taxa most commonly recorded from hills were Gorgonacea and Scleractinia. Bycatch from the two geographically separate groups of hills also differed significantly. 4. The largest bycatch volumes comprised corals from hills: Scleractinia (Goniocorella dumosa), Stylasteridae (Errina chathamensis) and Antipatharia (?Bathyplates platycaulus). Such large sessile epifauna may significantly increase the complexity of benthic habitat and trawling damage may thereby depress local biodiversity. Coral patches may require 4100 yr to recover. 5. Other environmental effects of deep-water trawling are briefly reviewed. 6. There is an urgent need to assess more fully the impact of trawling on seamount biotas and, in consequence, possible conservation measures. -
Ecological Characterization of Bioluminescence in Mangrove Lagoon, Salt River Bay, St. Croix, USVI
Ecological Characterization of Bioluminescence in Mangrove Lagoon, Salt River Bay, St. Croix, USVI James L. Pinckney (PI)* Dianne I. Greenfield Claudia Benitez-Nelson Richard Long Michelle Zimberlin University of South Carolina Chad S. Lane Paula Reidhaar Carmelo Tomas University of North Carolina - Wilmington Bernard Castillo Kynoch Reale-Munroe Marcia Taylor University of the Virgin Islands David Goldstein Zandy Hillis-Starr National Park Service, Salt River Bay NHP & EP 01 January 2013 – 31 December 2013 Duration: 1 year * Contact Information Marine Science Program and Department of Biological Sciences University of South Carolina Columbia, SC 29208 (803) 777-7133 phone (803) 777-4002 fax [email protected] email 1 TABLE OF CONTENTS INTRODUCTION ............................................................................................................................................... 4 BACKGROUND: BIOLUMINESCENT DINOFLAGELLATES IN CARIBBEAN WATERS ............................................... 9 PROJECT OBJECTIVES ..................................................................................................................................... 19 OBJECTIVE I. CONFIRM THE IDENTIY OF THE BIOLUMINESCENT DINOFLAGELLATE(S) AND DOMINANT PHYTOPLANKTON SPECIES IN MANGROVE LAGOON ........................................................................ 22 OBJECTIVE II. COLLECT MEASUREMENTS OF BASIC WATER QUALITY PARAMETERS (E.G., TEMPERATURE, SALINITY, DISSOLVED O2, TURBIDITY, PH, IRRADIANCE, DISSOLVED NUTRIENTS) FOR CORRELATION WITH PHYTOPLANKTON -
Bioluminescence and Fluorescence of Three Sea Pens in the North-West
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.08.416396; this version posted December 9, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Bioluminescence and fluorescence of three sea pens in the north-west Mediterranean sea Warren R Francis* 1, Ana¨ısSire de Vilar 1 1: Dept of Biology, University of Southern Denmark, Odense, Denmark Corresponding author: [email protected] Abstract Bioluminescence of Mediterranean sea pens has been known for a long time, but basic parameters such as the emission spectra are unknown. Here we examined bioluminescence in three species of Pennatulacea, Pennatula rubra, Pteroeides griseum, and Veretillum cynomorium. Following dark adaptation, all three species could easily be stimulated to produce green light. All species were also fluorescent, with bioluminescence being produced at the same sites as the fluorescence. The shape of the fluorescence spectra indicates the presence of a GFP closely associated with light production, as seen in Renilla. Our videos show that light proceeds as waves along the colony from the point of stimulation for all three species, as observed in many other octocorals. Features of their bioluminescence are strongly suggestive of a \burglar alarm" function. Introduction Bioluminescence is the production of light by living organisms, and is extremely common in the marine environment [Haddock et al., 2010, Martini et al., 2019]. Within the phylum Cnidaria, biolumiescence is widely observed among the Medusazoa (true jellyfish and kin), but also among the Octocorallia, and especially the Pennatulacea (sea pens). -
Adaptations for Survival: Symbioses, Camouflage & Mimicry
Adaptations for Survival: Symbioses, Camouflage & Mimicry OCN 201 Biology Lecture 11 http://www.berkeley.edu/news/media/releases/2005/03/24_octopus.shtml Symbiosis • Parasitism - negative effect on host • Commensalism - no effect on host • Mutualism - both parties benefit Often involves food but benefits may also include protection from predators, dispersal, or habitat Parasitism Leeches (Segmented Worms) Tongue Louse (Crustacean) Nematodes (Roundworms) Commensalism or Mutualism? Anemone shrimp http://magma.nationalgeographic.com/ Anemone fish http://www.scuba-equipment-usa.com/marine/APR04/ Mutualism Cleaner Shrimp and Eel http://magma.nationalgeographic.com/ Whale Barnacles & Lice What kinds of symbioses are these? Commensal Parasite Camouflage • Often important for predators and prey to avoid being seen • Predators to catch their prey and prey to hide from their predators • Camouflage: Passive or adaptive Passive Camouflage Countershading Sharks Birds Countershading coloration of the Caribbean reef shark © George Ryschkewitsch Fish JONATHAN CHESTER Mammals shiftingbaselines.org/blog/big_tuna.jpg http://www.nmfs.noaa.gov/pr/images/cetaceans/orca_spyhopping-noaa.jpg Passive Camouflage http://www.cspangler.com/images/photos/aquarium/weedy-sea-dragon2.jpg Adaptive Camouflage Camouflage by Accessorizing Decorator crab Friday Harbor Marine Health Observatory http://www.projectnoah.org/ Camouflage by Mimicry http://www.berkeley.edu/news/media/releases/2005/03/24_octopus.shtml Mimicry • Animals can gain protection (or even access to prey) by looking -
Food Web Lesson Plan
NYSDEC Region 1 Freshwater Fisheries I FISH NY Program Food Web Grade Level(s): 3-5 NYS Learning Standards Time: 30-45 minutes Core Curriculum MST Group Size: 10-30 Living Environment: Standard 4 Students will: understand and apply Summary scientific concepts, principles, and theories Students will be introduced to some of the pertaining to the physical setting and organisms in an aquatic ecosystem. The concept living environment and recognize the of food webs and the many roles organisms play historical development of ideas in science. as consumers, producers, and decomposers will • Key Idea 5: Organisms maintain a be introduced. Students will participate in an dynamic equilibrium that sustains activity to learn how humans play a role in the life. aquatic food web as anglers and consumers. • Key Idea 6: Plants and animals depend on each other and their Objectives physical environment. • Students will be able to identify 1-3 fish specific to fishing site • Students will be able to construct an aquatic food web • Students will be able to explain how humans play a role in the aquatic food web • Students will be able to identify species as producers, consumers, or decomposers Materials o Organism Identification Cards o Food Web worksheet o Fish mounts/pictures of fish o Suggested Organism Props for each identification card: . Angler: fishing rod with thick fishing line . Crab: tongs . Plankton: hair band with springs . Sun: sunglasses . Algae: toothpaste or plastic fish tank plant . Bird: noise maker or feathers . Bait: air freshener . Shellfish: fake pearl necklace . Fish: models, pictures, or nose plugs . Skate: elbow & knee pads .